Bushra Ismail

The interaction of a model active pharmaceutical with cationic surfactant and the subsequent design of drug based ionic liquid surfactants

Interactions of active pharmaceutical ingredients (API) with surfactants remain an important research area due to the need to improve drug delivery systems. In this study, UV-Visible spectrophotometry was used to investigate the interactions between a model low molecular weight hydrophilic drug sodium valproate (SV) and cationic surfactant cetyltrimethylammonium bromide (CTAB). Changes in the spectra of SV were observed in pre- and post-micellar concentrations of CTAB. The binding constant (Kb) values and the number of drug molecules encapsulated per micelle were calculated, which posed the possibility of mixed micelle formation and strong complexation between SV and CTAB. These results were compared to those of a novel room temperature surface active ionic liquid, which was synthesized by the removal of inorganic counterions from a 1:1 mixture of CTAB and SV. In this new compound the drug now constitutes a building block of the carrier and, as such, has considerably different surfactant properties to its building blocks. In addition, enhanced solubility in a range of solvents, including simulated gastric fluid, was observed. The study provides valuable experimental evidence concerning the performance of drug based surfactant ionic liquids and how their chemical manipulation, without altering the architecture of the API, leads to control of surfactant behavior and physicochemical properties. In turn, this should feed through to improved and controlled drug release rates and delivery mechanisms, and the prevention of precipitation or formation of polymorphs typical of crystalline form APIs.

Sonochemically synthesized green sorbent for the simultaneous removal of trace metal ions: application and estimation of measurement uncertainty through bottom-up approach

Polyethyleneimine functionalized eggshell membrane (ESM–PEI) as a green biosorbent has been successfully utilized for the removal of toxic metals. ESM–PEI was sonochemically synthesized by cross-linking amine/amide functional groups of ESM with PEI using glutaraldehyde as a cross-linker. This overall functionalization was carried out in an ultrasonic bath. Surface modification of ESM–PEI was confirmed by Fourier transform infrared spectroscopy and scanning electron microscopy. All analytes were easily extracted by the ESM–PEI packed cartridge followed by spectrometric determination. After successful functionalization, the adsorption capacity of ESM–PEI improved almost 25 times over that of ESM. Different variables affecting the extraction efficacy were investigated. Under optimum conditions, the ESM–PEI packed cartridge showed good stability even after >70 adsorption/desorption cycles run while maintaining over 96% analyte recoveries. Validity of the proposed procedure was checked with certified reference materials as well as by assessing its precision (RSD values < 20%) and trueness (relative error < 11%) under day-to-day conditions. The developed procedure has been further validated by following ISO/IEC 17025 recommendations considering the possible uncertainties through a “bottom-up” approach. The proposed procedure was successfully applied to the environmental water samples for the extraction of Cu, Pb, Cd, and Ni, where ESM–PEI was found to be an environmentally friendly, economic, and more rugged biosorbent.

Adsorption Assisted Photocatalytic Removal of Methyl Orange by MgAl2O4-Sb2S3 Composite Material

BACKGROUND The current article is about the water treatment in which colored water contaminated by methyl orange has been used for adsorption assisted photocatalysis. Coupling of photocatalysis with the traditional water treatment processes has been in practice since last couple of years for the improvement of degradation efficiencies, for example, photocatalysis coupled with ultrafilteration, adsorption, flocculation, biological methods, photolysis, membrane distillation, etc. Among all these coupling approaches, adsorption assisted photocatalysis being a very simple and highly efficient approach is suffering from few drawbacks on the account of high cost, low stability and surface area of the adsorbent support. The present study is a contribution towards improvement in this coupling approach. A low cost, highly stable spinel magnesium aluminate (MgAl2O4) material synthesized at nanoscale is used for composite formation with antimony sulphide (Sb2S3) material having high absorption coefficient in the visible light of solar spectrum. A review of recent patents shows that the field of photoctalysis is dominated by the traditional TiO2 catalyst. The modification of TiO2 by either composite formation or by doping is the main focus. METHODS Coprecipitation method is used for the synthesis of spinel in which the desired precursors in the respective molar ratios were mixed and annealing of the resulting precipitates was carried out at 800oC for 8 h. Sb2S3 was synthesized by the hydrothermal method in which the required molar solution of precursors was mixed with urea solution and the whole mixture was maintained at 105oC for 6 hrs in a Teflon lined autoclave. The resulting suspension was then annealed at 37oC for 3 hours. The composite of Sb2S3 and MgAl2O4 has been synthesized by mixing both the materials in 1:1 and heat treated in an oven at a temperature of 200oC. RESULTS Peaks in X-ray diffraction pattern correspond to both the Sb2S3 and spinel phase. All the peaks corresponding to the Sb2S3 and spinel phase were found to be shifted to higher d-spacing values. This indicates the expansion of unit cells of the Sb2S3 and MgAl2O4 phases. Thermal studies show that only 3% weight loss is observed at a temperature of 200- 1000oC which may be due to the loss of surface water from the sample. Surface area, pore volume and pore size obtained from N2 adsorption were 143m2/g, 0.21cc/g and 23.26Å, respectively. The removal efficiency of 0.1g catalyst for methyl orange solution of 5mg/L concentration after reaction in dark conditions for the time of one hour was calculated to be 24% owing to the adsorption. The visible light degradation efficiency of the 0.1g catalyst for 1, 5, 19, 25 and 50 mg/L concentrations of MO solutions were 97, 93, 75, 72 and 62% respectively. The dosage of the catalyst was found to have a direct relationship with the degradation efficiency. Lower pH was found suitable for the degradation owing to better interaction of catalyst surface and the adsorbed dye. Percent degradation increased with the increase in the time and temperature of reaction. The degradation kinetics followed pseudo first order rate equation; the calculated value of rate constant was 0.0102 min-1. CONCLUSION The mechanism involves the excitation of electrons in the valence band of Sb2S3 to the conduction band by the absorption of visible and UV light. The electrons and holes participate in the surface reactions resulting in the formation of superoxide and hydroxyl radicals which degrade the targeted polluted. Lower concentration of MO solutions, acidic pH, higher catalyst dosage and greater reaction times were found suitable for the degradation efficiency.

Comparative Studies on the Use of Binary and Ternary Combinations of Various Acidifying Agents for the Reduction of Soil pH

ABSTRACT The present study deals with the effects of addition of sulfur along with other acidifying agents for their ability to lower and maintain the pH in a given range for a longer period of time. The chemicals were subjected to batch test individually and in combinations. Treatments were applied to three soils of different textures: sandy clay loam, clay loam, and silt loam. A 1:1 soil/water paste along with the added amendment was maintained at room temperature for 2 months. Most of the chemical treatments lowered the pH significantly. Combinations containing S/Al2(SO4)3/H2SO4, S/Al2(SO4)3/H2O2, and S/H2O2/H2SO4 were found to be very effective in lowering the pH. The soil pH remained acidic for 2 months, indicating the suitability of chemically amended soil for the plantations requiring acidic soil pH.